Exchange of marine sodium for calcium during chemical weathering in the Isle aux Morts River basin,Newfoundland

Seasalt corrections applied to major-ion data for the Isle aux Morts River, Newfoundland, using Cl^? as the seawater indicator species, produce numerous negative values of Na⁺ that occur chiefly in the winter, when the seasalt concentrations are high. The negative values of Na⁺ are accompanied by slightly higher than usual concentrations of Ca⁺⁺, suggesting an exchange reaction of the form: $\text{Ca}\text{silicate}\text{+ 2 Na}{}^{\mathrm{+}}\text{= Na}{}_2\text{silicate}\text{+ Ca}{}^{\mathrm{++}}$, that is driven by seasalt.That the river receives seasalt inputs of normal major-ion seawater composition is indicated by analysis of precipitation chemistry data for nearby coastal stations.     

Hydrothermal systems in peridotites at slow-spreading ridges. Modeling phase transformations and material balance: Role of gabbroids

This work was aimed on the estimation of role of gabbro in the ore mobilization during hydrothermal transformation of oceanic (gabbro-peridotite) crust at slow-spreading mid-ocean ridges. Kinetic-thermodynamic modeling was used to reconstruct the geochemical and mineralogical trends of evolution of gabbroids during their hydrothermal interaction with marine fluid. The results of our simulation offered a new insight into some problems of material balance and ore formation during hydrothermal process in the slow-spreading mid-ocean ridges. It was shown that the root zones of all known MAR hydrothermal fields related to serpentinites are made up of ultrabasic rocks and located within peridotite protolith near hot and uncooled gabbroic bodies. It was also demonstrated that the observed mineral and geochemical diversity of metagabbros of slow-spreading mid-ocean ridges was provided by the interaction of hydrothermal fluid percolating through the Hess-type oceanic crust with gabbro bodies. It was established that almost cooled gabbroid bodies, being involved in hydrothermal circulation in the shallow root zones, may play an important role in the redistribution of the material within the Hess-type oceanic crust.     

Formation of tonalite in island arcs by seawater-induced anatexis of mafic rocks; evidence from the Lyngen Magmatic Complex, North Norwegian Caledonides

The Lyngen Magmatic Complex (LMC) of North Norway, consists of a western suite of layered gabbros of normal-mid oceanic ridge basalt (N-MORB) affinity and an eastern suite of layered gabbronorites, quartz-bearing gabbros and diorites/quartz-diorites of IAT (island-arc tholeiitte) to boninitic affinity. The boundary between the suites is defined by a large-scale ductile shear zone, the Rypdalen shear zone (RSZ). In this shear zone anatectic tonalites were generated by partial melting of the gabbro in the presence of an H₂O bearing fluid phase.Quartz from the tonalites contains early secondary and secondary liquid-dominated inclusions (88-99 wt.% H₂O), with an average salinity of 18 wt.% (calculated as NaCl_eq). Combined gas and ion chromatography shows that the major ions in the fluid are Cl⁻, Ca²⁺, Na⁺ with smaller amounts of K⁺, Mg²⁺, Sr²⁺, Br⁻ and NO₃⁻. The dominant non-H₂O volatile species is N₂ (0.5-10%), and small amounts of CO₂, CH₄ and other hydrocarbons are also present.The cation concentrations in the fluid are variable, due to element exchange during interaction of the fluids with the tonalites, amphibolites and metagabbros of the RSZ. The fluid contributed Na⁺ and K⁺ to the melt and gained Ca²⁺ in exchange, explaining the variable Na⁺/Ca²⁺ ratio of the fluid. The Br⁻ and Cl⁻ contents of the fluid inclusions plot on the same line as evaporating sea water, which strongly suggests a seawater origin for the fluid phase, and a seawater source fits well with other geochemical signatures and the tectonic setting of the LMC.It is suggested that seawater escaped from a subducting slab and was channelled along the Rypdalen shear zone. This caused anatexis of the gabbro, generating tonalitic melts at 0.5-0.9 GPa and 680-800°C.     

洋中脊热液系统中的锇及其同位素

洋中脊热液系统是将相对富集在深部的Os运移到海底表面的重要媒介,同时该过程也是全球Os循环的重要组成部分.在归纳总结洋中脊热液系统各物源组分和产物中Os的化学形态、含量及其同位素组成特征的基础上,探讨了Os在洋中脊热液活动各阶段中的分布演化规律及物源贡献特征.在缺乏沉积物覆盖的洋中脊区域,热液系统中的Os及其同位素组成特征主要受控于海水和不同构造环境下洋壳组分特征的差异以及这两种物源组分混合比例的不同.经历了海底之下的水岩反应后,围岩会将下渗海水中的部分放射性成因Os固定,而将自身富集的非放射性成因Os释放进入热液流体中.堆积在海底之上的各种热液产物中的Os大多来自海水,而海底之下的热液产物则因为海水下渗深度以及海水与热液流体混合程度的差异而体现出宽泛的Os含量和187Os/188Os比值变化范围.      

Carbonatization of oceanic crust by the seafloor hydrothermal activity and its significance as a CO2 sink in the Early Archean

Early Archean (3.46 Ga) hydrothermally altered basaltic rocks exposed near Marble Bar, eastern Pilbara Craton, have been studied in order to reveal geological and geochemical natures of seafloor hydrothermal carbonatization and to estimate the CO₂ flux sunk into the altered oceanic crust by the carbonatization. The basaltic rocks are divided into basalt and dolerite, and the basalt is further subdivided into type I, having original igneous rock textures, and type II, lacking these textures due to strong hydrothermal alteration. Primary clinopyroxene phenocrysts are preserved in some part of the dolerite samples, and the alteration mineral assemblage of dolerite (chlorite + epidote + albite + quartz ± actinolite) indicates that the alteration condition was typical greenschist facies. In other samples, all primary minerals were completely replaced by secondary minerals, and the alteration mineral assemblage of the type I and type II basalts (chlorite + K-mica + quartz + carbonate minerals ± albite) is characterized by the presence of K-mica and carbonate minerals and the absence of Ca-Al silicate minerals such as epidote and actinolite, suggesting the alteration condition of high CO₂ fugacity. The difference of the alteration mineral assemblages between basalt and dolerite is probably attributed to the difference of water/rock ratio that, in turn, depends on their porosity.Carbonate minerals in the carbonatized basalt include calcite, ankerite, and siderite, but calcite is quite dominant. The δ¹³C values of the carbonate minerals are −0.3 ± 1.2‰ and mostly within the range of marine carbonate, indicating that the carbonate minerals were formed by seafloor hydrothermal alteration and that carbonate carbon in the altered basalt was derived from seawater. Whole-rock chemical composition of the basaltic rocks is essentially similar to that of modern mid-ocean ridge basalt (MORB) except for highly mobile elements such as K₂O, Rb, Sr, and Ba. Compared to the least altered dolerite, all altered basalt samples are enriched in K₂O, Rb, and Ba, and are depleted in Na₂O, reflecting the presence of K-mica replacing primary plagioclase. In addition, noticeable CO₂ enrichment is recognized in the basalt due to the ubiquitous presence of carbonate minerals, but there was essentially neither gain nor loss of CaO. This suggests that the CO₂ in the hydrothermal fluid (seawater) was trapped by using Ca originally contained in the basalt. The CaO/CO₂ ratios of the basalt are generally the same as that of pure calcite, indicating that Ca in the basalt was almost completely converted to calcite during the carbonatization, although Mg and Fe were mainly redistributed into noncarbonate minerals such as chlorite.The carbon flux into the Early Archean oceanic crust by the seafloor hydrothermal carbonatization is estimated to be 3.8 × 10¹³ mol/yr, based on the average carbon content of altered oceanic crust of 1.4 × 10^-3 mol/g, the alteration depth of 500 m, and the spreading rate of 1.8 × 10¹¹ cm²/yr. This flux is equivalent to or greater than the present-day total carbon flux. It is most likely that the seafloor hydrothermal carbonatization played an important role as a sink of atmospheric and oceanic CO₂ in the Early Archean.     

Calculation of multicomponent chemical equilibria and reaction processes in systems involving minerals,gases and an aqueous phase

The compositional characteristics of many geochemical systems which involve the interaction of natural aqueous solutions with minerals and gases are conveniently described using the following thermodynamic components: Cl^?, SO₄⁼, HS^?, CO₃⁼, H⁺, Na⁺, K⁺, Ca⁺⁺, Mg⁺⁺, Fe⁺⁺, Zn⁺⁺, Cu⁺, Al⁺⁺⁺, SiO₂ and H₂O. A set of mass balance and mass action equations equal in number to the number of components plus the number of saturated minerals (and gases) is defined for a specified temperature, pressure and bulk composition. The mass balance equations include terms for minerals, gases and the molalities of aqueous complexes and dissociated species. This set of non-linear equations can be solved with the aid of a computer using'a Newton-Raphson technique. The calculation takes account of aqueous ion complexing, oxidation-reduction equilibria, activity coefficients, non-unit water activity and solid solutions. The use of H⁺, SO₄⁼, HS^? and H₂O as components allows straightforward treatment of processes involving oxidation-reduction, evaporation, boiling and changes of total aqueous H⁺ due to hydrolysis, mineral reaction or temperature change. One product of this approach is a technique for calculating pH at high temperature from measurement of pH at room temperature.By linking a series of discrete overall heterogeneous equilibrium calculations in which incremental changes of bulk composition, temperature or pressure are made, dynamic geochemical processes can be modeled. Example calculations for two such processes are given. These are the heating of seawater from 25° to 300°C and the isothermal irreversible reaction of rhyolite with an aqueous solution at 250°C.     

Geochemical assessment of groundwater around Macherla-Karempudi area,Guntur district,Andhra Pradesh

Groundwater in Palnad sub-basin is alkaline in nature and Na⁺-Cl⁻-HCO₃⁻ type around Macherla-Karempudi area in Guntur district, Andhra Pradesh. Total dissolved solids (TDS) show strong positive correlation with Cl⁻, Na⁺, Ca²⁺ and Mg²⁺, and positive correlation with SO₄²⁻, K⁺ and HCO₃⁻. Calcareous Narji Formation is the dominant aquifer lithology, and water-rock interaction controls the groundwater chemistry of the area. Chloro-alkaline indices (CAI) are positive at Miriyala, Adigopula, Mutukuru, Macherla and Durgi suggesting replacement of Na⁺ and K⁺ ions from water by Mg⁺⁺ and Ca⁺⁺ ions from country rock through base exchange reactions. Negative CAI values are recorded at Terala, Rayavaram and Nehrunagar, which indicate exchange of Na⁺ and K⁺ from the rock as cation-anion exchange reaction (chloro-alkaline disequilibrium). TDS range from 91 to 7100 ppm (Avg. 835 ppm) and exceed the prescribed limit of drinking water around Mutukuru, Durgi, Rayavaram, Khambampadu and Ammanizamalmadaka areas. Scanty rainfall and insufficient groundwater recharge are the prime factors responsible for high salinity in the area. Fluoride content ranges from <1 to 3.8 ppm and contaminated areas were identified around Macherla (1 sq km; 3.8ppm), Mandadi (1 sq km, 2.1ppm) and Adigopula (2 sq km, <1 to 3.7 ppm). The % Na⁺ content varies from 17 to 85 with the mean value of 57, and eighty (80) samples showed higher %Na⁺ in comparison to the prescribed limit of 60 for irrigation water. Sodium Adsorption Ratio (SAR) and % Na⁺ in relation to total salt concentration indicate that groundwater (51%) mostly falls under doubtful to poor quality for irrigation purpose. Groundwater of Adigopula village is fluoride contaminated and remedial measures are suggested to improve the water quality.     

Ocean floor metamorphism in the Betts Cove ophiolite,Newfoundland

The mineralogical and geochemical features of the lower Ordovician Betts Cove ophiolite of northeastern Newfoundland indicate that hydrothermal circulation of seawater near a mid-ocean ridge has been involved in the metamorphism of the complex. The degree of greenschist facies metamorphism increases with stratigraphie depth in the ophioli te. Calcite, hematite and epidote distributions show that the metamorphosing fluid penetrated downward and was reduced with depth. The mobilities of major and trace elements support the hypothesis of the interaction of seawater and basalt: Fe₂O₃, MgO, Na₂O and H₂O increase whereas CaO and Cu decrease in the rock after alteration; SiO₂, total iron, K₂O, Ba and Rb can either be depleted or enhanced in the altered material; TiO₂, P₂O₅, Zr, Y, Cr and Ni remain stable during the metamorphic episode. Finally, the occurrence of massive sulphides and incipient rodingitic gabbro is explicable in a circulatory seawater system.     

Modelling the geochemical cycle of boron: Implications for the long-term δ11B evolution of seawater and oceanic crust

The boron geochemical cycle has been simulated using a time-dependent geochemical box model that was coupled to a one-dimension model of seawater–oceanic crust interactions. Boron elemental and isotopic compositions of oceanic rocks as a function of depth were calculated by mass balance, using the temperature and porosity profiles of the crust as well as the available experimental and empirical distribution coefficients and fractionation factors between mineral and water. Ranges of boron elemental and isotopic variations of seawater were calculated for crust–seawater interactions that take place from the ridge-axis to the off-axis closure of the hydrothermal system. The present-day δ¹¹B of seawater (40‰) could represent a steady-state value. However, depending on crustal permeability, lifetime of water–rock interactions, and expansion rate of the oceanic ridge, the δ¹¹B of seawater may vary from 30‰ to 50‰ at the 10 million year scale.Some boron isotope compositions of Cretaceous biogenic carbonates and ophiolitic serpentinites from Oman are comparable to modern rock samples, suggesting that the δ¹¹B of Cretaceous seawater was close to the present-day value. Low δ¹¹B values of some biogenic carbonates cannot be attributed to low pH values of past seawater, but more probably to δ¹¹B variations of seawater or diagenetic alteration by crustal aqueous fluids. Boron isotope composition of hydrothermally altered serpentines could be considered as a promising proxy of the seawater composition.     

Oceanic plagiogranites as a result of interaction between magmatic and hydrothermal systems in the slow-spreading mid-ocean ridges

The paper considers some petrological and geochemical aspects of the formation of oceanic plagiogranites (OPG)—felsic intrusive rocks, which were found in the plutonic complexes of modern mid-ocean ridges (MOR) and ophiolites of paleo-collisional zones. Based on the multi-equilibrium clinopyroxene-orthopyroxene-amphibole-plagioclase geothermobarometry, typical OPG found in gabbros and peridotites were formed at temperatures of 820–850°C and pressure of 2–2.5 kbar. Close temperature estimates (825 ± 50°C) were obtained from literature data on Ti content in zircon, with allowance for lowered TiO₂ activity in the rock. Under these P-T parameters, OPG can be generated only in the presence of fluid of water activity $ \left( {a_{H_2 O} } \right) $ \left( {a_{H_2 O} } \right) close to 0.9. OPG and associated recrystallized gabbroids contain high-temperature hornblende with significant Cl content (0.5–2 wt %). In addition, the plagiogranites are characterized by particular geochemical features such as extremely high Na₂O/K₂O (up to 135), sharp LREE enrichment ((Ce/Yb)_cn and (La/Sm)_cn up to 10 and 4, respectively), and elevated ⁸⁷Sr/⁸⁶Sr ratio relative to DMM. All these facts point to the key role of hydrothermal fluid, the seawater derivative, in the OPG formation. The fluid with $ a_{H_2 O} = 0.9 $ a_{H_2 O} = 0.9 (approximately 28 wt % NaCl) could be produced from seawater due to hydration reactions at the higher lower temperature horizons of oceanic crust in the course of its percolation to the OPG generation areas. The formation of plagiogranites in the MOR oceanic core complexes possibly reflects the fundamental feature of oceanic accretion: practically simultaneous (at the geological time scale) proceeding of exogenic (neptunic) and endogenous (plutonic) processes.     

Groundwater chemistry and occurrence of arsenic in the Meghna floodplain aquifer,southeastern Bangladesh

Dissolved major ions and important heavy metals including total arsenic and iron were measured in groundwater from shallow (25–33 m) and deep (191–318 m) tube-wells in southeastern Bangladesh. These analyses are intended to help describe geochemical processes active in the aquifers and the source and release mechanism of arsenic in sediments for the Meghna Floodplain aquifer. The elevated Cl⁻ and higher proportions of Na⁺ relative to Ca²⁺, Mg²⁺, and K⁺ in groundwater suggest the influence by a source of Na⁺ and Cl⁻. Use of chemical fertilizers may cause higher concentrations of NH₄⁺ and PO₄³⁻ in shallow well samples. In general, most ions are positively correlated with Cl⁻, with Na⁺ showing an especially strong correlation with Cl⁻, indicating that these ions are derived from the same source of saline waters. The relationship between Cl⁻/HCO₃⁻ ratios and Cl⁻ also shows mixing of fresh groundwater and seawater. Concentrations of dissolved HCO₃⁻ reflect the degree of water–rock interaction in groundwater systems and integrated microbial degradation of organic matter. Mn and Fe-oxyhydroxides are prominent in the clayey subsurface sediment and well known to be strong adsorbents of heavy metals including arsenic. All five shallow well samples had high arsenic concentration that exceeded WHO recommended limit for drinking water. Very low concentrations of SO₄²⁻ and NO₃⁻ and high concentrations of dissolved Fe and PO₄³⁻ and NH₄⁺ ions support the reducing condition of subsurface aquifer. Arsenic concentrations demonstrate negative co-relation with the concentrations of SO₄²⁻ and NO₃⁻ but correlate weakly with Mo, Fe concentrations and positively with those of P, PO₄³⁻ and NH₄⁺ ions.     

The equilibration of clay minerals with sea water: exchange reactions

Studies of seawater-sediment and seawater-clay mineral exchange equilibria demonstrate that rinsing procedures employed in many previous studies have grossly shifted the exchange equilibria away from the true seawater conditions. Exchange complements have been determined here by measurement of compositional changes in seawater that result from reaction with clays, thereby avoiding rinsing. These data show that exchangeable Na⁺ is normally greater than or equal to exchangeable Mg²⁺ on clays and sediments in exchange equilibrium with seawater.On introduction to seawater, fluvial clays are shown to give up their exchangeable Ca²⁺ for Na⁺, a process of importance in the geochemical budget of Na⁺.     

北祁连缝合带油葫芦沟玄武岩地球化学特征

对油葫芦沟蛇绿岩中玄武岩进行了地球化学研究, 以探讨其形成环境。油葫芦沟蛇绿岩中玄武岩的主量和微量元素具有低钾富钠的特征, 属低钾(拉斑)系列。玄武岩的球粒陨石标准化稀土元素分配模式图表现为近平坦型, 轻重稀土富集不明显, 属于亏损地幔(N型)。大离子亲石元素(LILE)Rb、K和Sr出现负异常, 高场强元素(HFSE)Nb、Ta、Hf、Zr无负异常, 表现出大洋中脊幔源岩浆作用的特征。构造环境判别图显示, 油葫芦沟玄武岩属于典型的亏损型大洋中脊玄武岩(MORB)。研究结果表明油葫芦沟蛇绿岩中玄武岩为北祁连洋洋壳的组成部分, 北祁连洋在晚元古代—晚寒武世为典型的大洋中脊环境。      

LIP Reading: Recognizing Oceanic Plateaux in the Geological Record

Basaltic oceanic plateaux are important features in the geologicalrecord. Not only do they record ancient mantle plume activity,but they also are believed to be important building blocks inthe formation of the continental crust. In this paper we reviewthe salient features of two Cretaceous oceanic plateaux (theOntong Java and the Caribbean–Colombian): thick sequencesof predominantly homogeneous basalt; the occurrence of high-MgObasalt, including komatiites; and an apparent absence of sheeteddyke complexes. In addition, pyroclastic deposits may be scarce.We then explore ways of distinguishing plateaux from basalticsequences erupted in different tectonomagmatic settings: continentalflood basalt provinces; island arcs; back-arc basins; oceanislands and mid-ocean ridges. Using these criteria, potentialArchaean and Proterozoic oceanic plateaux are reviewed and identified.Finally, we explore how these remnant oceanic plateaux becameincorporated into the continents, by reviewing the proposedaccretion mechanisms for the Cretaceous Caribbean–Colombianoceanic plateau, on the basis of evidence from South Americaand the tonalites of the southern Caribbean island of Aruba. KEY WORDS: oceanic plateau; basalt geochemistry; large igneous provinces; plumes     

Chemical exchange during hydrothermal alteration of basalt by seawater—II. Experimental results for Fe,Mn, and sulfur species

Fresh mid-ocean ridge basalts of varying crystallinity and an andesite were reacted with seawater and with a Na-K-Ca-Cl solution at 200–500°C and 500–1000 bar in sealed gold capsules. $\text{Water}\text{rock}$ mass ratios of one to three were used and durations ranged from two to twenty months. The concentrations of Fe, Mn, and reduced and oxidized sulfur species in solution reached steady state in most of the experiments at 400–500°C, but not in those at 200–300°. The concentrations of Fe and Mn were a few ppm at 200–300° and increased greatly with temperature between 300 and 500°. The low values at 200–300° are probably related to the uptake of Fe and Mn by smectite at the in situ pH, which was slightly acid at 200° and slightly alkaline at 300°. The quench pH values decreased with increasing temperature above 300°. The only reliable data for the concentration of Zn in solution were obtained at 400°, where values 1–2 ppm were found. Copper was extensively leached from basalt and andesite and was deposited as part of a Cu-Au alloy in the capsule walls or, in some experiments, as chalcopyrite.Reduced sulfur was readily leached from basalt into solution, and was also produced by the reduction of seawater sulfate by ferrous iron derived from the basalts. The proportion of seawater sulfate which was reduced in the experiments with a $\text{water}\text{rock}$ ratio of one varied from 5–10% at 300°C to > 95% at 500°. The rate of sulfate reduction depended on the run temperature, on the crystallinity and initial sulfur content of the rocks used as starting materials, and on the $\text{water}\text{rock}$ ratio. The final concentration of reduced sulfur in solution increased greatly with temperature, and generally exceeded that of Fe on a molal basis.The oxide-sulfide assemblages produced in the experiments resemble those in the basalt-seawater geothermal system at Reykjanes, Iceland, and in hydrothermally altered basalts and gabbros from the oceanic crust; they include pyrite, pyrrhotite. chalcopyrite, hematite, and probably magnetite. The particular assemblage varied systematically with the temperature, rock type, and crystallinity of each run. Anhydrite precipitated in all experiments with seawater, at all temperatures from 200–500°C. However, its persistence to the end of the runs was apparently metastable, as it should have reacted with the final solutions to produce pyrite or pyrrhotite.     

Reach-Scale Cation Exchange Controls on Major Ion Chemistry of an Antarctic Glacial Meltwater Stream

McMurdo dry valleys of Antarctica represent the largest of the ice-free areas on the Antarctic continent, containing glaciers, meltwater streams, and closed basin lakes. Previous geochemical studies of dry valley streams and lakes have addressed chemical weathering reactions of hyporheic substrate and geochemical evolution of dry valley surface waters. We examine cation transport and exchange reactions during a stream tracer experiment in a dry valley glacial meltwater stream. The injection solution was composed of dissolved Li⁺, Na⁺, K⁺, and Cl^-. Chloride behaved conservatively in this stream, but Li⁺, Na⁺, and K⁺ were reactive to varying degrees. Mass balance analysis indicates that relative to Cl^-, Li⁺ and K⁺ were taken up in downstream transport and Na⁺ was released. Simulations of conservative and reactive (first-order uptake or generation) solute transport were made with the OTIS (one-dimensional solute transport with inflow and storage) model. Among the four experimental reaches of Green Creek, solute transport simulations reveal that Li⁺ was removed from stream water in all four reaches, K⁺ was released in two reaches, taken up in one reach, and Na⁺ was released in all four reaches. Hyporheic sediments appear to be variable with uptake of Li⁺ in two reaches, uptake of K⁺ in one reach, release of K⁺ in two reaches, and uptake of Na⁺ in one reach. Mass balances of the conservative and reactive simulations show that from 1.05 to 2.19 moles of Li⁺ was adsorbed per reach, but less than 0.3 moles of K⁺ and less than 0.9 moles of Na⁺ were released per reach. This suggests that either (1) exchange of another ion which was not analyzed in this experiment or (2) that both ion exchange and sorption control inorganic solute transport. The elevated cation concentrations introduced during the experiment are typical of initial flows in each flow season, which flush accumulated dry salts from the streambed. We propose that the bed sediments (which compose the hyporheic zone) modulate the flushing of these salts during initial flows each season, due to ion exchange and sorption reactions.     

内蒙古月牙山蛇绿岩的岩石学、地球化学特征及其地质意义

内蒙古月牙山蛇绿岩分布于红柳河-洗肠井蛇绿岩带东部的月牙山一带,出露较完整,自下而上由超基性杂岩、辉长岩、层状玄武岩和枕状玄武岩及放射虫硅质岩组成。岩石学、岩石化学、地球化学资料显示,蛇绿岩套中的主要单元均源于幔源,接近于现代洋壳蛇绿岩特征。与蛇绿岩单元伴生的斜长花岗岩属于幔源型大洋斜长花岗岩,且为蛇绿岩组成的一部分;辉长岩、玄武岩均形成于正常洋中脊(N-MORB)环境。     

Environmental research of groundwater in the urban and suburban areas of Attica region,Greece

In this study, 92 groundwater samples were collected from the Attica region (Greece). Moreover, geographical information system database, geochemistry of groundwater samples and statistics were applied. These were used for studying the chemical parameters (NO₃ ⁻, Mg²⁺, Ca²⁺, Cl⁻, and Na⁺) and conductivity spatial distribution and for assessing their environmental impact. The ranges of chemical parameters of the water samples (in mg L⁻¹) are: NO₃ ⁻ 1–306, Mg²⁺ 2–293, Ca²⁺ 3–453, Cl⁻ 5–1,988, and Na⁺ 4–475. The elevated concentrations of sodium, Mg²⁺, Cl⁻ are attributed to natural contamination (seawater intrusion). On the other hand, NO₃ ⁻ elevated concentrations are attributed to anthropogenic contamination (nitrate fertilizers). The results of the GIS analysis showed that elevated values of Na⁺, Mg²⁺, Cl⁻ are related to shrubby and sparsely vegetated areas, while elevated values of NO₃ ⁻ are connected with urban and agricultural areas.     

Groundwater chemical and fecal contamination assessment of the Jerba unconfined aquifer,southeast of Tunisia

Located in the southeast of Tunisia, on the Mediterranean Sea, Jerba Island has a semiarid climate condition. The surface water scarcity has made groundwater the main source to supply the domestic, touristic, and agricultural water demand. Unconfined aquifer is a vulnerable costal aquifer system that undergoes several phenomena. This work aims at assessing the geochemical and bacteriological groundwater quality, defining groundwater pollution sources and promoting sustainable development and effective management of groundwater resources in Jerba Island. Data were collected after the wet season in 2014 from 79 wells. Electric conductivity, pH, TDS, and major and fecal tracers (total coliforms, thermotolerant coliforms, Escherichia coli, and Salmonella) were analyzed. Geochemical modeling including the relationships between geochemical tracers Na⁺ vs. Cl^?, Ca²⁺ vs. Cl^?, K⁺ vs. Cl^?, representative ionic ratios (Br^?/Cl^?, Na⁺/Cl^?, Mg²⁺/Ca²⁺), and statistical analysis were used to specify major process contributing to groundwater pollution and main factors controlling groundwater mineralization in the island. Groundwater varieties were hydrochemically classified into three types in terms of salinity values: group 1 (8.86%) to fresh water, group 2 (27.84%) to brackish water, and group 3 (63.29%) belongs to saline water. In addition, groundwater quality revealed high concentrations in chemical pollution tracers (Na⁺, Cl^?, SO₄ ^2?, and NO₃ ^?) and fecal tracers. Besides, most of the sampled wells were contaminated with nitrate (50.63%). Also, thermotolerant coliforms and E. coli were detected in all groundwater samples (96.2% of wells). Results indicated that the Jerba shallow aquifer was under serious threat from both natural and anthropogenic contamination. However, the wild discharge of domestic effluents, septic tanks, and sewage were the main origins of underground water contamination in Jerba Island. The reduction of fecal sources, through constructing normalized latrines is thus recommended.